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  2. Organic thiocyanates - Wikipedia

    en.wikipedia.org/wiki/Organic_thiocyanates

    In methyl thiocyanate, N≡C and C−S distances are 116 and 176 pm. By contrast, N=C and C=S distances are 117 and 158 pm in isothiocyanates. [7] Typical bond angles for C−S−C are 100°. [3] By contrast C−N=C in aryl isothiocyanates is 165°. Again, the thiocyanate isomers are quite different with C−S−C angle near 100°.

  3. Transition metal complexes of thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Transition_metal_complexes...

    Thiocyanate complexes are not widely used commercially. Possibly the oldest application of thiocyanate complexes was the use of thiocyanate as a test for ferric ions in aqueous solution. [15] The reverse was also used: testing for the presence of thiocyanate by the addition of ferric salts. The 1:1 complex of thiocyanate and iron is deeply red.

  4. Thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Thiocyanate

    Thiocyanate shares its negative charge approximately equally between sulfur and nitrogen. As a consequence, thiocyanate can act as a nucleophile at either sulfur or nitrogen—it is an ambidentate ligand. [SCN] − can also bridge two (M−SCN−M) or even three metals (>SCN−

  5. Table of standard reduction potentials for half-reactions ...

    en.wikipedia.org/wiki/Table_of_standard...

    Definitions must be clearly expressed and carefully controlled, especially if the sources of data are different and arise from different fields (e.g., picking and directly mixing data from classical electrochemistry textbooks (versus SHE, pH = 0) and microbiology textbooks (′ at pH = 7) without paying attention to the conventions on which ...

  6. Bridging ligand - Wikipedia

    en.wikipedia.org/wiki/Bridging_ligand

    The interchange of bridging and terminal ligands is called bridge-terminal exchange. The process is invoked to explain the fluxional properties of metal carbonyl and metal isocyanide complexes. [6] Some complexes that exhibit this process are cobalt carbonyl and cyclopentadienyliron dicarbonyl dimer: Co 2 (μ-CO) 2 (CO) 6 ⇌ Co 2 (μ-CO) 2 (CO ...

  7. Hypothiocyanite - Wikipedia

    en.wikipedia.org/wiki/Hypothiocyanite

    It is formed when an oxygen is singly bonded to the thiocyanate group. Hypothiocyanous acid is a fairly weak acid; its acid dissociation constant (pK a) is 5.3. Hypothiocyanite is formed by peroxidase [1] catalysis of hydrogen peroxide and thiocyanate: H 2 O 2 + SCN − → OSCN − + H 2 O

  8. Rosenkranz double - Wikipedia

    en.wikipedia.org/wiki/Rosenkranz_double

    The Rosenkranz double and Rosenkranz redouble are elements of a bridge bidding convention invented by Dr. George Rosenkranz, collectively known as the Rosenkranz double. [1] It is a double made by the advancer (partner of the overcaller) in an auction where opener, overcaller and responder have all bid different suits. It is used to describe ...

  9. Copper(I) thiocyanate - Wikipedia

    en.wikipedia.org/wiki/Copper(I)_thiocyanate

    Copper(I) thiocyanate is a hole conductor, a semiconductor with a wide band gap (3.6 eV, therefore transparent to visible and near infrared light). [11] It is used in photovoltaics in some third-generation cells as a hole transfer layer.